ライフサイエンスコーパス: transport protein

1 t of serum albumin, the extracellular Cu(2+) transport protein.

2 ansporter G family member40, encoding an ABA transport protein.

3 e and one lacking the relevant SbmA membrane transport protein.

4 Stard7, an intracellular phosphatidylcholine transport protein.

5 stulate that STM2200 functions as a specific transport protein.

6 s/cholesterol moieties onto this large lipid transport protein.

7 of the SLC25A40 inner mitochondrial membrane transport protein.

8 e inhibitors to access Fe(3+) from a primary transport protein.

9 ne/threonine protein kinases, and a putative transport protein.

10 t nonbiphasic high-affinity nitrate-specific transport protein.

11 al residues of different classes of specific transport proteins.

12 ort facilitated by plasma membrane-localized transport proteins.

13 isite to understand the function of membrane transport proteins.

14 ase require vesicular and/or plasma membrane transport proteins.

15 sequence of CAII, a region that binds other transport proteins.

16 the combined actions of a range of membrane transport proteins.

17 used to measure expression levels of key ion transport proteins.

18 ENV nonstructural protein 5 and host nuclear transport proteins.

19 pathway constitutes a unique mechanism among transport proteins.

20 l of CP110 and recruitment of intraflagellar transport proteins.

21 s found within the subunits of many membrane transport proteins.

22 F-hand mitochondrial SCaMCs buffering/solute transport proteins.

23 so is limited evidence for a role of glucose transport proteins.

24 munication in this important family of Cl(-) transport proteins.

25 enzymes, transcription factors, and membrane transport proteins.

26 g of various transmembrane receptors and ion-transport proteins.

27 n heme binding and release in bacterial heme transport proteins.

28 mes and the BetX and CbcXWV quaternary amine transport proteins.

29 ts can competitively bind to thyroid hormone transport proteins.

30 to detect conformational changes in ammonium transport proteins.

31 he picture of Cbl interaction with its three transport proteins.

32 ecific and reversible inhibition of membrane transport proteins.

33 nitrite transporter (FNT) family of membrane transport proteins.

34 ng secondary active Na(+)-dependent membrane transport proteins.

35 ircular plasmid 26 (cp26), encode key purine transport proteins.

36 this large and important family of membrane transport proteins.

37 of a miR cluster targeting a family of metal transport proteins.

38 ds able to restore function to faulty copper transport proteins.

39 modifying, intracellular trafficking and RNA transport proteins.

40 the host importin (IMP) alpha/beta1 nuclear transport proteins.

41 lacenta richly expresses nonheme and heme Fe transport proteins.

42 manner that depends on FA type and cellular transport proteins.

43 G nucleoporins induced by the cargo-carrying transport proteins.

44 lular localization of PIN-FORMED (PIN) auxin transport proteins.

45 ulin stimulates the translocation fatty acid transport protein 1 (FATP1) to plasma membrane, and thus

46 ts the erythrocyte sugar transporter glucose transport protein 1 (GLUT1) and examines the transporter

47 d translocase CD36 (R(2) = 0.30), fatty acid transport protein 1 (R(2) = 0.24), and AcylCoA synthetas

48 , fatty acid-binding protein, and fatty acid transport protein 1 were measured.

49 spho-EPRS binds SLC27A1 (that is, fatty acid transport protein 1, FATP1), inducing its translocation

50 of two types of accessory proteins, receptor transporting protein 1 short and odorant binding protein

51 We found that receptor transporting protein 1 short enhanced the membrane expre

52 in WDR35, encoding retrograde intraflagellar transport protein 121 (IFT121), in three families with a

53 is a hypomorphic mutation of intraflagellar transport protein 172 (Ift172), required for ciliogenesi

54 of (99m)Tc-mebrofenin through organic anion transport protein 1a and 1b (Oatp1a/1b) and multidrug re

55 g and Ag(+), expression levels of the Copper Transport Protein 2 (CTR2) indicated that Ag biouptake c

56 ere, we provide evidence that intraflagellar transport protein 20 (IFT20) interacts with E3 ubiquitin

57 We showed previously that the intraflagellar transport protein 20 (IFT20), a component of the intrafl

58 eation, Golgi distribution of intraflagellar transport protein 20 homologue, and ciliogenesis.

59 Fatty acid transport protein 4 (FATP4) is one of a family of six tr

60 n fatty acids-like 1 (ELOVL1) and fatty acid transport protein 4 (FATP4), which each have very long-c

61 1; and the fatty acid transporter fatty acid transport protein 4 have all been linked to AD.

62 variant observed in the gene Intraflagellar Transport Protein 43 (IFT43) was studied by heterologous

63 inhibitors of the liver-specific fatty acid transport protein 5 (FATP5).

64 ntly inhibited mRNA expression of fatty acid transport protein 5 in the presence of DGLA, which was i

65 terolemia induced an important change in HDL-transported proteins (576 spots in HL-HDL vs. 621 spots

66 at SDCCAG3 interacts with the intraflagellar transport protein 88 (IFT88), a crucial component of cil

67 kinesin family member 3a and intraflagellar transport protein 88, proteins that are essential for ci

68 rogressive synaptic, cytoskeletal and axonal transport protein abnormalities that may accompany the d

69 s uses the Type VII ESX secretion systems to transport proteins across its complex cell wall.

70 ll bacteria use the conserved Sec pathway to transport proteins across the cytoplasmic membrane, with

71 y little is known about the translocons that transport proteins across the two membranes that surroun

72 tein translocon is a multimeric complex that transports proteins across lipid bilayers.

73 nergic neurons and asked how inactivation of transport proteins affected iron homeostasis in vivo in

74 ture; IFT, in contrast, might be required to transport proteins against cellular concentration gradie

75 key endosomal sorting complexes required for transport proteins Alix or TSG101) exhibit similar pause

76 ated that hepcidin is complexed to the blood transport protein, alpha2-macroglobulin (alpha2M).

77 nexpected molecular link between a vesicular transport protein and a syndrome of autoimmunity manifes

78 include the demonstration of intraflagellar transport protein and hedgehog contributions to the immu

79 Similar to LbtU, LbtP is a siderophore transport protein and is required for robust growth unde

80 cture is currently available for any nitrate transport protein and the mechanism by which nitrate is

81 ated with increased levels of intraflagellar transport proteins and accelerated ciliogenesis in neona

82 Alcohol exposure up-regulated fatty acid transport proteins and caused lipid accumulation in the

83 aled increased levels of carbon fixation and transport proteins and decreased levels of ammonia oxida

84 on, higher expression of ammonia and nitrite transport proteins and key metabolic enzymes mainly in t

85 Vesicular carriers transport proteins and lipids from one organelle to anot

86 Coat protein II (COPII)-coated vesicles transport proteins and lipids from the endoplasmic retic

87 T)-A, IFT-B, and the BBSome], which together transport proteins and other molecules along the cilium.

88 Assigning function to orphan membrane transport proteins and prioritizing candidates for detai

89 ce of regulated trafficking through specific transport proteins and routes.

90 icate outside pathogens and thus express few transport proteins and thus few surface epitopes for hos

91 SCRT (endosomal sorting complex required for transport) proteins and found that ESCRT II and IV signi

92 Owing to the ubiquitous presence of ion transport-proteins and cell-cell heterogeneity in biolog

93 ormation of axonal varicosities sequestering transported proteins and progressive neuronal cell death

94 ole in intercellular signaling in mammals by transporting proteins and small RNAs.

95 ng, localization of PIN-FORMED1 (PIN1) auxin transport proteins, and in situ hybridization of leaf de

96 ractions with regulators of gene expression, transport proteins, and metabolic pathways.

97 herichia coli, TatBC complexes recognize the transported proteins, and TatA complexes are recruited t

98 We show here that the ROS-regulated Ca(2+) transport protein Annexin 1 in Arabidopsis thaliana (AtA

99 Here we uncover a novel role of Cu transport protein Antioxidant-1 (Atox1), which is origin

100 mount and the localization of these membrane transport proteins appears as a way to drive their activ

101 Plasma membrane-localized transport proteins are internalized through endocytosis

102 t in B. subtilis and that the other putative transport proteins are likely to be utilized for more-sp

103 Among the smallest known transport proteins are members of the small multidrug re

104 dramatically decreased whereas other copper transport proteins are not altered.

105 r, the mechanisms regulating the location of transport proteins are still largely unknown.

106 he genes encoding sodium-dependent vitamin C transport proteins are strongly associated with plasma a

107 Major facilitator superfamily (MFS) transport proteins are ubiquitous in the membranes of al

108 sCOPT1, which encodes a high-affinity copper transport protein, as well as other copper-deficiency ma

109 , a member of the importin family of nuclear transport proteins, as an intracellular binding partner

110 H7 has been shown to express heme uptake and transport proteins, as well as use heme as an iron sourc

111 Transthyretin (TTR) is a homotetrameric transport protein, assembled from monomers that each con

112 lectrical contacts are made between electron transport proteins associated with the outer membranes o

113 of the regulation of water, urea, and sodium transport proteins; (b) better resolution of the anatomi

114 lt with pancreatic ductal adenocarcinoma and transport protein-based therapeutic and diagnostic conce

115 nd approximately 25% of prokaryotic membrane transport proteins belong to this superfamily.

116 has significant homology with several yeast transport proteins belonging to the major facilitator su

117 ntroduces variation in the activities of ion-transport proteins between cells.

118 ber of the Lipocalin family of extracellular transport proteins, binds to Wg with nanomolar affinity

119 We evaluated whether manganese transport protein C (MntC), which is conserved across th

120 Broad-spectrum inhibitors of ABC transport proteins can be of great use in cancers that s

121 zation of FG nucleoporin assemblies with the transport proteins can be understood within a first prin

122 ic endomembrane compartments and polar auxin transport protein cargoes.

123 motor expressed in inner ear hair cells that transports protein cargos within developing mechanosenso

124 paradigm for the largest family of membrane transport proteins, catalyzes the coupled translocation

125 paradigm for the largest family of membrane transport proteins, catalyzes the coupled translocation

126 intracellular distribution of the fatty acid transport protein, CD36, altering fatty acid metabolism.

127 mide phosphoribosyl transferase or in the NR transport protein, CD73.

128 By exploiting the ability of a natural heme transport protein, ChuA, to promiscuously import heme de

129 TCDB is the only transport protein classification database adopted by the

130 rotein (BCRP, ABCG2) are the three major ABC transport proteins conferring resistance to many structu

131 s, we suggest that related cases of membrane transport proteins containing similar motifs are widespr

132 Solute carrier (SLC) membrane transport proteins control essential physiological funct

133 alled PCSK9 and Sec24A, a well known protein-transport protein, could lead to the development of nove

134 Moreover, knockdown copper transport protein, Ctr1, also inhibited CoCl2-induced EM

135 osides upon reconstitution with the electron transport proteins cytochrome b5 and NADH-cytochrome b5

136 el membrane protein LptD (lipopolysaccharide transport protein D) translocates LPS from the periplasm

137 inding protein (NikE), periplasmic dipeptide transport protein (DppA), and outer membrane protein A (

138 tic Sec61 translocon was able to efficiently transport proteins entirely composed of intrinsically di

139 Hemoglobin (Hb) is the heme-containing O2 transport protein essential for life in all vertebrates.

140 rum albumin has an established function as a transport protein, evidence is emerging that serum album

141 quaporin 1 (AQP1) is a plasma membrane water-transporting protein expressed strongly in tumor microva

142 igned to analyze the distinctive features of transport proteins, extending its usefulness.

143 Fatty acid transport protein (FATP) 4 is one of a family of six FAT

144 2, beta enolase and glycogen phosphorylase), transport proteins (fatty acid-binding protein, myoglobi

145 cherichia coli ferric citrate outer-membrane transport protein FecA has been characterized; little is

146 round the crystal structure of this membrane transport protein, followed by atomistic simulations.

147 inding protein 4 (RBP4) is the sole specific transport protein for retinol in the blood, but it is al

148 rmed samt-1, coding for a candidate membrane transport protein for the presumptive donor substrate of

149 etic mechanisms may generally denote primary transport proteins for bacteria.

150 cell populations, and require intraflagellar transport proteins for their formation.

151 r binding sites on transthyretin (TTR), a T4 transport protein found in plasma and cerebrospinal flui

152 two mitochondrial preprotein and amino acid transport proteins from Arabidopsis thaliana, NADH dehyd

153 y is directed by cargo-bearing vesicles that transport proteins from one compartment to another.

154 s, because it provides a mechanism to remove transport proteins from the membrane.

155 tion of BBS proteins in photoreceptors is to transport proteins from the OS to the cell body or to pr

156 nt of coat protein complex II (COPII), which transports proteins from the endoplasmic reticulum (ER)

157 a hereditary or acquired deficiency of iron-transporting protein function that diminishes transmembr

158 cently, we established that these two sodium transport proteins functionally interact in the second p

159 e propose that COPT2, a high-affinity copper transport protein, functions under copper and iron defic

160 The human blood-brain barrier glucose transport protein (GLUT1) forms homodimers and homotetra

161 ates that are putative substrates of glucose transport proteins (GLUTs) and possess hypoxia-selective

162 However, the identity of heme transport proteins has been elusive.

163 A complex network of zinc import and transport proteins has evolved to control zinc concentra

164 endipitous discovery the CLC family of Cl(-) transporting proteins has been a never ending source of

165 Amino acid transport proteins have been shown to be upregulated in

166 opic changes, including altered abundance of transport proteins having AAA-ATPase motifs.

167 None of these mutations occurred in transport protein homologues; instead, they affected hou

168 lysis of an artificial hexacoordinate oxygen transport protein, HP7, which operates via a mechanism s

169 ions in solution, using testosterone and its transport proteins human serum albumin (HSA) and sex hor

170 Intraflagellar transport proteins (IFT) are required for hedgehog (Hh)

171 which encodes the retrograde intraflagellar transport protein IFT139, cause both isolated nephronoph

172 we conditionally deleted the intraflagellar transport protein Ift88 (Ift88(-/fl)).

173 a hypomorphic mutation in the intraflagellar transport protein IFT88 (Ift88Tg737Rpw mice, also known

174 o required for recruiting the intraflagellar transport proteins Ift88 and Ift52 to the mother centrio

175 e role of alpha-synuclein and other cellular transport proteins implicated in PD and how their aberra

176 We previously identified a peroxisomal transport protein in Arabidopsis (Arabidopsis thaliana)

177 loride cotransporter, NCC, is the major NaCl transport protein in the distal convoluted tubule (DCT).

178 tive abundance of key mitochondrial electron transport proteins in 263K-infected animals relative to

179 the abundance of transcripts encoding auxin transport proteins in an ETR1 and EIN2 (ethylene signali

180 the potential of expressing desired membrane transport proteins in cell factories to achieve the expo

181 Aquaporins are a large family of water transport proteins in cell membranes.

182 membrane localization of multiple bile salt transport proteins in central hepatocytes and may act as

183 he role proposed for the apolipophorin lipid transport proteins in Hedgehog and Wnt movement.

184 as an ion exchanger through manipulation of transport proteins in the cell membrane.

185 significantly smaller, and expression of key transport proteins in the epithelial cells lining this r

186 The crowded electron transport proteins in the periplasm of the organism cons

187 ignificant changes in other water- or sodium-transporting proteins in the gene-modified mice.

188 ce and phosphorylation of other renal sodium-transporting proteins, including NaPi-IIa, NKCC2, and EN

189 evidence has suggested that these two sodium transport proteins interact.

190 n beta, a well established nucleocytoplasmic transport protein, interacts with components of the retr

191 ated with contrasting cellular phenotype, to transport proteins into the mitochondria.

192 While the ensemble of ion transport proteins involved in cell volume regulation is

193 , notably in SLC genes that include membrane transport proteins involved in the transport of endogeno

194 d the uptake through a high-affinity uranium transport protein involving the modification of the uran

195 This transport protein is a major target to overcome multidru

196 A ligand-loaded transport protein is immobilized on the solid support, a

197 The principal active yeast ion transport protein is the plasma membrane H(+)-ATPase.

198 irment of nuclear HR23 and nucleocytoplasmic transport proteins is an outcome of, and a contributor t

199 rent understanding of these specific silicon transport proteins is limited by the lack of in vitro st

200 rs, it has been shown that a subset of these transport proteins is regulated by magnesium-responsive

201 and H(+) translocation with secondary active transport proteins is the identification and physical lo

202 Transferrin, an iron transport protein, is a clinically important biomarker i

203 erved, along with accumulation of the axonal transport proteins JNK-interacting protein 1 and amyloid

204 Iron-bound legiobactin is imported by the transport protein LbtU.

205 expression of the ATP-binding cassette (ABC) transport proteins, like ABCG2, triggering active efflux

206 OM by an unknown mechanism involving the LPS transport proteins, LptA-G.

207 entified a highly conserved family of sterol transport proteins (Ltc/Lam) localized at diverse MCSs.

208 ipid-synthesizing, lipid-flippase, and lipid-transport proteins (LTPs) collaborate to control lipid b

209 amin E for common binding sites within lipid transport proteins may alter the traffic of lipid mediat

210 Here, we elucidated which transport proteins mediate the hepatic uptake of conjuga

211 nregulated, and Ca2+-dependent mitochondrial transport proteins MIRO1 and KIF5C were reduced.

212 arbon metabolism, photosynthesis, metabolite transport, protein modification, cell wall remodeling, a

213 lone protein, but together with the electron transport proteins NADH-cytochrome b5 reductase (CYB5R)

214 the structure of a bacterial nitrate/nitrite transport protein, NarK, from Escherichia coli, with and

215 rric heme iron center in the NO-storage and -transport protein Nitrophorin 2 (NP2) from the salivary

216 Such a dual use of transport proteins not only enables efficient substrate

217 a gene reporter, based on the organic anion transporting protein Oatp1a1, which mediates uptake of a

218 er Mhp1 is a sodium-coupled secondary active transport protein of the nucleobase-cation-symport famil

219 Here, we demonstrate the use of a class of transport proteins of pharmacological interest to circum

220 comprehensive genetic analysis of 35 orphan transport proteins of Plasmodium berghei during its life

221 Several bacterial ion-transporting proteins or their auxiliary subunits posses

222 studies show that inhibition of the hepatic transport proteins organic anion-transporting polypeptid

223 appc11gene, which encodes a component of the transport protein particle (TRAPP) complex.trappc11mutan

224 The transport protein particle (TRAPP) complexes activate Ra

225 Originally identified in yeast, transport protein particle (TRAPP) complexes are Rab GTP

226 nd mass spectrometry, we determined that the transport protein particle (TRAPP) II complex associates

227 The large multisubunit transport protein particle (TRAPP) II complex has been p

228 The transport protein particle (TRAPP) III complex, comprisi

229 The oligomeric complex transport protein particle I (TRAPPI) mediates nucleotid

230 Here we show that transport protein particle III (TRAPPIII), a conserved a

231 as well as the major facilitator superfamily transport protein PcaK.

232 enase (HemO) along with the cytoplasmic heme transport protein PhuS control heme flux into the cell.

233 A subclass of bacterial CLC anion-transporting proteins, phylogenetically distant from lon

234 amyloplasts and relocalization of the auxin transport protein, PIN3.

235 Besides these transport proteins, plant-specific polyphenolic compound

236 Mitochondrial structural and transport proteins play an important role in the develop

237 a novel role that MOG1, a nucleocytoplasmic transport protein, plays in cardiac physiology and devel

238 a to the gut lumen depends on the epithelial transport protein, polymeric immunoglobulin receptor (pI

239 Transport proteins previously described in maturation am

240 sduction, starch and sucrose metabolism, RNA transport, protein processing in endoplasmic reticulum,

241 of MUC1-ED with both NEU1 and its chaperone/transport protein, protective protein/cathepsin A.

242 SCRT (endosomal sorting complex required for transport) protein recruitment at the level of individua

243 idney require an overlapping set of membrane transport proteins regulated by the forkhead transcripti

244 Because other iron-transport proteins remain active, labile iron gradients

245 (MDR) mediated by ATP-binding cassette (ABC) transport proteins remains a major problem in the chemot

246 TrkH belongs to a superfamily of K(+) transport proteins required for growth of bacteria in lo

247 s a freely accessible reference database for transport protein research, which provides structural, f

248 abase serves as a common reference point for transport protein research.

249 TCDB) serves as a common reference point for transport protein research.

250 e attributed to alterations in the vitamin A-transport proteins retinol-binding protein 4 (RBP4) and

251 (Rho) tags and/or chaperones (i.e. Receptor Transporting Protein, RTP1S, Ric8b and G(alphaolf)) to i

252 complex with SatPC and specific phospholipid transport protein(s) to initiate trafficking of SatPC fr

253 nslation of the mRNA coding for the selenium transport protein, selenoprotein P (SELENOP), which in v

254 han those of the protein chromophores) using transport proteins (serum albumins and alpha1-acid glyco

255 p foci is reduced in the absence of the mRNA-transport protein She3, suggesting that unphosphorylated

256 A soluble sterol transport protein, STARD4, accounts for approximately 25

257 trieval is mediated by the activity of sugar transport proteins (STPs).

258 he method of MD, we use a number of membrane transport proteins studied in our laboratory as examples

259 ved in metabolic functions, stress response, transport, protein synthesis, and DNA repair.

260 ABCB11 is a canalicular transport protein that controls the rate-limiting step i

261 er, to date no report exists on any specific transport protein that facilitates Cam uptake.

262 SERCA is a membrane transport protein that has been extensively studied.

263 (NPF) 6.3 is a dual-affinity plasma membrane transport protein that has both high- and low-affinity f

264 zyme IIC (EIIC) is a membrane-embedded sugar transport protein that is part of the phosphoenolpyruvat

265 ctively, these data identify ZIP8 as an iron transport protein that may function in iron metabolism.

266 broadly distributed and precisely controlled transport protein that mediates volume and pH regulation

267 (Protein interacting with C kinase 1), is a transport protein that regulates the trafficking of ion

268 MlaA represents a lipid transport protein that selectively removes outer leaflet

269 onstrate that mitochondria express a calcium transport protein that shares characteristics with the N

270 uire Ca(2)(+) influx through plasma membrane transport proteins that are regulated by reactive oxygen

271 Membrane transport proteins that catalyse arsenic uptake by roots

272 A) transport across the ciliary body and the transport proteins that may contribute.

273 Kinesins are motor-based transport proteins that play diverse roles in various ce

274 n homeostasis is maintained by iron and heme transport proteins that work in concert with ferrireduct

275 Seven LPS transport proteins (that is, LptA-LptG) form a trans-env

276 such, understanding how the two main sodium transport proteins, the thiazide-sensitive sodium chlori

277 a involves the coupling of an outer membrane transport protein to the transperiplasmic protein TonB.

278 close proximity of sterol esterification and transport proteins to each other combined with their res

279 This cellular exchange of sugars requires transport proteins to mediate uptake or release from cel

280 lar biofilms were enriched in outer membrane transport proteins to scavenge the extracellular milieu

281 s a nucleus and the machinery to express and transport proteins to subcellular locations.

282 RT (endosomal sorting complexes required for transport) proteins to induce the formation of vesicle (

283 w details are revealed about the system that transports proteins to the tip of flagella during growth

284 he 776C-->G polymorphism of the vitamin B-12 transport protein transcobalamin gene (TCN2) (rs1801198;

285 Cbl transport is mediated by three transport proteins: transcobalamin, intrinsic factor, an

286 e proteins, including, for nonheme iron, the transport protein transferrin and the intracellular iron

287 We show that the iron transport protein transferrin is engaged in ancient and

288 biorecognition element, recombinant thyroid transport protein transthyretin (rTTR), and dedicated mo

289 The tetrameric thyroxine transport protein transthyretin (TTR) forms amyloid fibr

290 reductants, and binding to human tocopherol transport protein (TTP).

291 overexpression of the mitochondrial membrane transport protein UCP2 in cancer cells is sufficient to

292 c acid treatment or by ablation of the lipid transport protein Ups1, both leading to an increase of m

293 n be found in many tyrosine kinase-regulated transport proteins using modified search programs, we su

294 In addition, cytoskeleton and membrane transport proteins were considerably altered during rege

295 and protein abundance of nonheme and heme Fe transport proteins were evaluated in placental tissue fr

296 otonin transporter (SERT) is a transmembrane transport protein which re-uptakes excessive 5-hydroxytr

297 he major facilitator superfamily of membrane transport proteins, which contain two domains of six tra

298 regulated by the mechanical stability of the transported protein, which determines both active nuclea

299 the defect we discovered that both the auxin transport protein ZmPIN1a and the squamosa promoter-bind

300 Mutations in the zinc efflux transport protein ZnT8 have been linked with both type 1